Question: What is the genetic association of the regulates (molecular biology) of the hsa-miR-6887-5p?
Paraphrase: What is the hereditary affiliation of the controls (atomic science) of the hsa-miR-6887-5p?
SPARQL (Wikidata): SELECT ?answer WHERE { wd:Q27593985 wdt:P128 ?X . ?X wdt:P2293 ?answer}
Answer: Alzheimer's disease, maturity-onset diabetes of the young, type 2 diabetes, permanent neonatal diabetes mellitus, maturity-onset diabetes of the young type 2, rare genetic diabetes mellitus, hyperinsulinism due to glucokinase deficiency, Epidermolysis bullosa simplex of Ogna, epidermolysis bullosa simplex with muscular dystrophy, autosomal recessive limb-girdle muscular dystrophy type 2Q, peroxisomal acyl-CoA oxidase deficiency, Crohn's disease, microcephaly 11, primary, autosomal recessive, congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome, hand-foot-genital syndrome, Guttmacher syndrome, migraine disorder, multiple sclerosis, age related macular degeneration, obesity, metabolic disease, Char syndrome, patent ductus arteriosus 2, complex cortical dysplasia with other brain malformations 5, prolactinoma, obesity, amyotrophic lateral sclerosis, hereditary sensory neuropathy type 1F, panic disorder, multiple sclerosis, neuroblastoma, spastic paraplegia-severe developmental delay-epilepsy syndrome, post-traumatic stress disorder, Van den Ende-Gupta syndrome, benign familial infantile epilepsy, Infantile convulsions and choreoathetosis, obesity, Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination, BIDS syndrome, autosomal dominant nonsyndromic deafness 44, congenital generalized lipodystrophy type 4